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The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohort.

Wan J, Pan H, Chang D, Zhao Y, Xu Q, Yao L, Sun Q, Zhang X, He R, Wang C, Zhang H, Lei L, Wang Y, Li M, Wu H, Ma J, Wu Y, Xu Y, Xiong N, Wang T, Wang X, Chen L, Xu Y, Cao H, Zhang K, Liu W, Zhang Y, Mao C, Wang Q, Xue Z, Zhang Z, Cheng O, Huang W, Zhao G, Cui G, Chen T, Wang P, Di W, Liu H, Zheng H, Chen C, Guo H, Xia K, Zhang Z, Yuan K, Li J, Wang J, Guo J, Shen L, Jiang H, Liu C, Liu J, Chan P, Liu Z, Tang B, Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC), China Essential Tremor Alliance (CETA).

NPJ Parkinsons Dis · 2026-03-28

DOI: 10.1038/s41531-026-01315-wPMID: 41904258

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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IFNγ alters the aberrant phenotype of α-synuclein-treated microglia reducing the detrimental impact of their secretome on dopaminergic neurons.

Niskanen J, Hakosalo V, Hämäläinen W, Kälvälä S, Hyvönen MT, Zhang Y, Luk KC, Koistinaho J, Lehtonen M, Goldsteins G, Albert K, Lehtonen Š.

Neuroscience · 2026-03-28

DOI: 10.1016/j.neuroscience.2026.03.040PMID: 41912064

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

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